Senior Real World Data Statistician I/II

Lead analytical strategies and statistical modelling for disease registries, natural history studies, EMR, and claims data to support global regulatory submissions.

Implement advanced statistical methods including survival analysis, causal inference, propensity score matching, and longitudinal modelling.

Draft statistical analysis plans, specifications, tables, figures, listings, and regulatory briefing documents in compliance with FDA RWE Framework and EMA guidelines.

Partner with clinical, epidemiology, regulatory, and external registry investigators to ensure data quality and methodological rigor.

Drive reproducibility, audit readiness, and transparent reporting for regulatory-grade real-world evidence generation.